Alconox Inc. is the leader in critical detergents since 1946 with top quality critical detergents used extensively in pharmaceutical, biotech, medical device, cosmetics, and healthcare facilities.
Quality Care: A trade name owned by MCAT for Ultrasound gel, and paste and cleaning gels for electrophysiological testing. Clients are governmental and private hospitals within Saudi Arabia directly or through NUPCO central purchasing.
GENERAL ACTIVITIES OF MCAT IN MEDICAL DEVICES SECTOR
B2B Shortages Fulfillment Service
This Service is dedicated to bridging the gap between supply and demand in the medical sector, ensuring essential healthcare products reach consumers promptly. In response to the critical shortages that can arise in the medical field, we’ve developed a responsive, efficient fulfillment process that prioritizes accessibility and timely delivery. Leveraging a robust supply chain network and advanced inventory management, we work directly with manufacturers and distributors to address shortages quickly and maintain a reliable supply of high-demand items. This service is designed to enhance patient care and support healthcare providers by ensuring that essential medical products are readily available when needed.
Regulatory Consultation Services:
Our regulatory consultation services are designed to guide medical and healthcare companies through the complex regulatory landscape. With an in-depth understanding of global regulatory standards and local compliance requirements, we help streamline the approval process for medical devices, pharmaceuticals, and cosmetic products. Our team of experienced regulatory consultants works closely with clients to develop tailored strategies that ensure compliance, reduce time to market, and mitigate risks. From regulatory submissions and audits to post-market surveillance and product registration, we provide end-to-end support to meet all regulatory needs, helping clients confidently bring their products to market and maintain compliance throughout their lifecycle.
Medical Devices Product Registration
Our Medical Devices Product Registration service ensures that your devices meet all regulatory requirements for successful market entry. Navigating the rigorous standards set by regulatory authorities can be challenging, and our dedicated team is here to simplify the process. With extensive expertise in regulatory frameworks across various markets, we manage all aspects of product registration—from documentation and compliance checks to regulatory submissions and approvals. Our streamlined approach minimizes delays and ensures that your medical devices are registered efficiently, allowing you to focus on innovation and growth while we handle the complexities of regulatory compliance.
